Increased bone formation and osteoblastic cell phenotype in premature cranial suture ossification (craniosynostosis)
Author:
Publisher
Wiley
Subject
Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism
Reference32 articles.
1. A genetic study of non syndromic coronal craniosynostosis;Lajeunie;Am J Med Genet,1995
2. Sutural biology and the correlates of craniosynostosis;Cohen;Am J Med Gen,1993
3. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis;Jabs;Cell,1993
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